Xu H - Search Results

1

Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing.

Guo Y, Yuan L, Yi J, Xiao J, Xu H, Lv H, Xiong W, Zheng W, Guan L, Zhang J, Xiang H, Qi Y, Deng H. Guo Y, et al. Among authors: xu h. Indian J Biochem Biophys. 2013 Aug;50(4):253-8. Indian J Biochem Biophys. 2013. PMID: 24772942

2

Genetic analysis of the NEUROG2 gene in patients with Parkinson's disease.

Deng S, Deng H, Le W, Xu H, Yang H, Deng X, Lv H, Xie W, Zhu S, Jankovic J. Deng S, et al. Among authors: xu h. Neurosci Lett. 2010 Jan 14;468(3):195-7. doi: 10.1016/j.neulet.2009.10.078. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879328

3

HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease.

Guo Y, Deng X, Zheng W, Xu H, Song Z, Liang H, Lei J, Jiang X, Luo Z, Deng H. Guo Y, et al. Among authors: xu h. Neurosci Lett. 2011 Sep 1;501(3):185-7. doi: 10.1016/j.neulet.2011.05.245. Epub 2011 Jul 20. Neurosci Lett. 2011. PMID: 21791235

4

Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease.

Guo Y, Lin H, Gao K, Xu H, Deng X, Zhang Q, Luo Z, Sun S, Deng H. Guo Y, et al. Among authors: xu h. Biochem Biophys Res Commun. 2011 Nov 18;415(2):284-7. doi: 10.1016/j.bbrc.2011.10.042. Epub 2011 Oct 18. Biochem Biophys Res Commun. 2011. PMID: 22027142

5

Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome.

Lei J, Deng X, Zhang J, Su L, Xu H, Liang H, Huang X, Song Z, Deng H. Lei J, et al. Among authors: xu h. Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):72-6. doi: 10.1002/ajmg.b.32003. Epub 2011 Nov 16. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22095709

6

No evidence of association between the LINGO4 gene and essential tremor in Chinese Han patients.

Liang H, Zheng W, Xu H, Lei J, Song Z, Jiang X, Zeng Z, Deng H. Liang H, et al. Among authors: xu h. Parkinsonism Relat Disord. 2012 Mar;18(3):303-5. doi: 10.1016/j.parkreldis.2011.10.017. Epub 2011 Nov 21. Parkinsonism Relat Disord. 2012. PMID: 22104011

7

Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD.

Guo Y, Deng X, Zhang J, Su L, Xu H, Luo Z, Deng H. Guo Y, et al. Among authors: xu h. Neurosci Lett. 2012 May 23;517(1):18-20. doi: 10.1016/j.neulet.2012.03.097. Epub 2012 Apr 9. Neurosci Lett. 2012. PMID: 22507240

8

Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome.

Guo Y, Su L, Zhang J, Lei J, Deng X, Xu H, Yang Z, Kuang S, Tang J, Luo Z, Deng H. Guo Y, et al. Among authors: xu h. Psychiatr Genet. 2012 Dec;22(6):300-3. doi: 10.1097/YPG.0b013e32835862b1. Psychiatr Genet. 2012. PMID: 22914617

9

Mutation screening of the HTR2B gene in patients with Tourette syndrome.

Guo Y, Deng X, Jankovic J, Su L, Zhang J, Le W, Xu H, Yang Z, Tang J, Kuang S, Deng H. Guo Y, et al. Among authors: xu h. Neurosci Lett. 2012 Sep 27;526(2):150-3. doi: 10.1016/j.neulet.2012.08.013. Epub 2012 Aug 14. Neurosci Lett. 2012. PMID: 22917605

10

Gene expression changes in peripheral blood from Chinese Han patients with Tourette syndrome.

Lei J, Xu H, Liang H, Su L, Zhang J, Huang X, Song Z, Le W, Deng H. Lei J, et al. Among authors: xu h. Am J Med Genet B Neuropsychiatr Genet. 2012 Dec;159B(8):977-80. doi: 10.1002/ajmg.b.32103. Epub 2012 Oct 17. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 23076970

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